CN108473834A

CN108473834A - Contact adhesive with filler

Info

Publication number: CN108473834A
Application number: CN201780007125.9A
Authority: CN
Inventors: 迪安·M·莫伦
Original assignee: 3M Innovative Properties Co
Current assignee: 3M Innovative Properties Co
Priority date: 2016-01-18
Filing date: 2017-01-06
Publication date: 2018-08-31
Also published as: US20210198534A1; EP3405541A1; WO2017127239A1; TW201739813A; US20190023948A1; KR20180101536A; JP2019505638A

Abstract

The present invention provides for contact adhesive and correlated product, the curable precurser composition of component and method.The composition provided contains (methyl) alkyl acrylate, hollow non-porous particulate filler and the surface modifier comprising hydrophobicity alkoxy silane or hydrophobicity organofunctional polysiloxane.These compositions and method make it possible in filler particles to be functionalized the filler particles in situ during or after with curable resin group subassembly, to allow than faster and producing more efficiently at pressure sensitive adhesive material when using conventional manufacturing method.

Description

Contact adhesive with filler

Technical field

The present invention provides with the relevant composition of contact adhesive, product, component and method.

Background technology

Contact adhesive (PSA) is that can be advantageously available for the viscoelastic material for being bonded to one another substrate.PSA is in different quotient Industry and industrial circle have wide applicability.Typical application be in strip product, commonly used in keeping, label, protection, The purpose of sealing and masking.

Known available PSA have certain characteristics, including aggressive tack and permanent adhesive, in the condition no more than finger pressure Under can bond, and to giving the enough interface binding intensity and cohesive bonding intensity of adherend.It is showed as PSA good Material is often engineered to show required viscoelastic polymer so that it is strong to there is viscosity, peel adhesion and shearing The appropriate balance of degree.Such material usually by such as (methyl) acrylate based polyalcohol and copolymer, natural rubber, synthesize rubber Glue and siloxanes are made.

For performance, cost and weight consider, can high expectations by certain particulate additives (or filler) incorporation PSA combination In object.Inorganic filler such as fumed silica particles can improve the physical characteristic of PSA tape material.As previously in PCT Publication number Described in WO 2014/186316 (Heimink et al.), other packing materials such as hollow glass microballoon or other hollow nothings Hole filler can also provide structure enhancing, reduce weight and cost, and also enhance peel strength and shear strength, especially as general When hollow glass microballoon is modified to include hydrophobic surface.Since the cost of hollow nonporous packing is less than the fluoropolymer resin of PSA Cost, therefore the manufacturing cost of band can be reduced.For the unit of weight of band be also in this way, its may be based on it is hollow The proportion of nonporous packing is less than the proportion of hardening (or solidification) fluoropolymer resin and is reduced.

Invention content

Technological challenge when sky nonporous packing is related to their minimum abrasive grains in use.Due to these fillers So small, they may be susceptible to become airborne, and makes modified, manipulation and become trouble comprising the problem of such material And it is difficult.Second Problem is will to be surface-treated the complex device being delivered to needed for filler particles, needs a large amount of time, money Sheet and other resources.Other procedure of processing is also commonly used for functionalization, cleaning, flushing and dry filler, this can cause to add Energy expenditure and solvent use.

This document describes by providing the filler during or after filler particles and curable resin group subassembly The in situ of grain is functionalized to eliminate or mitigate the composition and method of above-mentioned technical problem.This can be by using with hydrophobicity alkane Oxysilane or hydrophobicity organofunctional polysiloxane realize as the composition of surface modifier.These compositions and side Method allows the PSA ratios for the filler being modified from surface faster and to be more effectively carried out manufacture using when conventional manufacturing method.

In a first aspect, providing a kind of curable precurser composition.The curable precurser composition includes：(methyl) Alkyl acrylate；Hollow non-porous particulate filler；And include hydrophobicity alkoxy silane or the poly- silicon of hydrophobicity functional organic The surface modifier of oxygen alkane.

In second aspect, pressure-sensitive adhesive composition is provided by making the solidification of aforementioned curable precursor composition.

In the third aspect, a kind of pressure-sensitive adhesive assembly is provided, which includes back sheet；And the One pressure sensitive adhesive layer, first pressure sensitive adhesive layer include the aforementioned pressure-sensitive adhesive composition being arranged on back sheet.

In fourth aspect, a kind of method preparing contact adhesive is provided, the method includes：By (methyl) acrylic acid Arrcostab, hollow non-porous particulate filler and comprising hydrophobicity alkoxy silane or hydrophobicity organofunctional polysiloxane Surface modifier mixes, to provide curable precursor composition；And so that curable precurser composition is cured to provide pressure-sensitive Adhesive.

Specific implementation mode

The PSA of the disclosure is prepared by hollow non-porous particulate filler, and surface includes mainly silica.These silica Surface is subjected to the processing carried out using hydrophobicity alkoxy silane and/or hydrophobicity organofunctional polysiloxane, described hydrophobic Property alkoxy silane and/or hydrophobicity organofunctional polysiloxane and silicon dioxde reaction to provide hydrophobic surface modification. In this process, it is in the mistake for mixing the filler of curable precurser composition and curable resin component that surface, which is modified, Occur in journey or later rather than before.

Such contact adhesive can be by high-peeling strength and the combination of high shear force tolerance in various types of substrates.This A little advantages can obtain in the substrate including low-surface-energy (LSE), middle surface energy (MSE) and/or high surface energy (HSE) substrate. This be especially surprisingly found because LSE, MSE and HSE substrate typically exhibit entirely different surface chemistry and energy Amount.

" low-surface-energy substrate " refers to the substrate with the surface energy less than 34 dynes per centimeters.It is included in such material Be polypropylene, polyethylene (for example, high density polyethylene (HDPE) or HDPE) and polyacrylic blend (for example, polypropylene/second Alkene propylene diene monomer (PP/EPDM), thermoplastic polyolefin (TPO)).

" middle surface energy substrate " refer to have between 34 and 70 dynes per centimeters, typically 34 and 60 dynes per centimeters it Between, and the substrate of the surface energy more typically between 34 and 50 dynes per centimeters.It is polyamide to be included in such material 6 (PA6), acrylonitrile-butadiene-styrene (ABS) (ABS), makrolon (PC)/ABS blend, PC, polyvinyl chloride (PVC), polyamides Amine (PA), polyurethane (PUR), thermoplastic elastomer (TPE) (TPE), polyformaldehyde (POM), polystyrene, poly- (methyl methacrylate), Clear coat of the clear coat surface in particular for vehicle such as automobile and the coating surface and composite wood for commercial Application Expect such as fibre reinforced plastics.

" high surface energy substrate " refers to the surface more than 350 dynes per centimeters, more preferably greater than 400 dynes per centimeters The substrate of energy, and more typically refer to those of the surface energy being included between 400 and 1100 dynes per centimeters substrate. It is metallic substrates (such as aluminium, stainless steel) and glass to be included in such material.

Surface energy is usually measured by the Contact-angle measurement described in such as ASTM D7490-08.

After " hydrophobic surface modification " instruction is modified on suitable surface, the surface of hollow non-porous particulate filler is for pole Property substance, especially water have significantly reduced affinity.

Multilayer PSA components based on the disclosure can be adhered to motor vehicle body side form plastic in exemplary application, keep out the wind Rain item, road sign, business designaton, structure, electrical cabinet, shell, machine parts, terminal box or the back of the body for photovoltaic module Plate solution.Multilayer PSA components are particularly suitable for being bonded to low energy surface, such as polyolefin surfaces and varnish coat table Face.Multilayer PSA components disclosed herein can advantageously be bonded to motor vehicle varnish coat surface.

In some embodiments, one or more psa layers include hollow non-porous particulate filler, and surface is changed by surface Property agent such as hydrophobicity alkoxy silane, hydrophobicity organofunctional polysiloxane or they mixture provide hydrophobicity table Face is modified.

Allowed by reducing the total of PSA components using hollow non-porous particulate filler at least the first psa layer of PSA components Body weight/density and the consumption by reducing at least precursor composition of the first psa layer for being used to form PSA components generate Cost-effective PSA components.

In an advantageous embodiment, hollow non-porous microparticle material significantly hinders the resin Composition of precursor composition The clearance space generated at least the first psa layer by particle packing material is filled (such as by capillarity, absorption or suction Receive) ability.

Particular aspects-construction of above-mentioned PSA and PSA components, monomer, tackifier, plasticizer, crosslinking agent, draws hollow packing Hair agent, chain-transferring agent, other optional additives, polymerization, manufacturing method and application-will be described in further detail under now Under literary corresponding subhead.

Construction

Can be had in multiple suitable configurations based on intended application and desired characteristic according to PSA the and PSA components of the disclosure Either one or two of.

PSA for example, the form of monolayer constructions can be used, and is substantially made of the first psa layer.This monolayer packages Can be advantageously used for such as transition zone — that is, do not have backing double-sided adhesive band.

In terms of one alternative, the form of multi-ply construction can be used in the PSA components of the disclosure, and includes two or more Multiple superimposed layers-are for example, the first psa layer and adjacent layer such as back sheet and/or other psa layer.Adhesive multi-ply construction or Band can be used advantageously as double-layer adhesive band, and two objects are adhered to each other.For this paper back sheet can or It can not show at least part of PSA features.

When there are back sheet, common PSA components are three-layer structure, and wherein back sheet is interposed in two discrete psa layers Between.

About multilayer PSA components, the present disclosure is not limited to embodiments above.As an alternative, PSA components may include At least one middle layer between back sheet and one or more psa layers.These middle layers and back sheet can express out favorably Mechanical property, such as increase multilayer PSA components tear resistance or optical function, for example, light transmittance, reflection, color and mark Note.

In a specific aspect, middle layer includes polymer, and the polymer is selected from polyacrylate, polyurethane, polyene Hydrocarbon, polystyrene, polyamide, natural rubber, synthetic rubber and polyvinylpyrrolidone and their copolymer and mixing Object.

However, it is also possible to which one or more intermediate psa layers are by curable precurser composition system as described in the present disclosure At.Compared with psa layer, the formula of one or more middle layers may be the same or different.

Available back sheet can be by plastics (such as polypropylene (including biaxially oriented polypropylene), vinyl, poly- second Alkene, polyester (such as polyethylene terephthalate)), non-woven fabric (for example, paper, cloth, non-woven scrim), metal foil, Foam (for example, polyacrylic, polyethylene, polyurethane, neoprene) etc. is made.

In a specific embodiment, the PSA components of the disclosure are the form of multilayer PSA components, the multilayer PSA groups Part further includes second psa layer adjacent with the first psa layer.

In the case where multilayer PSA components further include second psa layer adjacent with the first psa layer, the multilayer PSA of the disclosure Component can advantageously take the form of table sheath core multilayer PSA components, wherein the first psa layer is the sandwich layer of multilayer PSA components, And the epidermis that the second psa layer is multilayer PSA components.Epidermis can extend in two main surfaces of sandwich layer and directly connect It touches.Such multilayer PSA components are well known.

In some embodiments, PSA components include the first psa layer, are foam of polymers.Term " polymer " foam " Refer to polymer material, it includes typically by volume at least 5%, by volume 10% to 55% or by volume 10% to The gap of 45% amount.

Gap or hole in polymer foam layer can be generated by any of method.Such method includes using gas Or other physical blowing agents and/or include hollow non-porous particle in the composition for polymer foam layer.For example, according to US A kind of method of generation foam of polymers described in 4,415,615, can obtain acrylic foam by following steps：(i) Make the composition foaming comprising acrylate monomer and optional comonomer, (ii) by foam-coating on backing, and (iii) composition of foaming is made to polymerize.The unexpanded composition of acrylate monomer and optional comonomer is coated to the back of the body It is possible to serve as a contrast and then blister simultaneously and polymerize the composition.The foaming of composition can by by gas stirring to polymerizable It is completed in composition.Preferred gas for this purpose is inert gas, such as nitrogen and carbon dioxide.

For this paper polymer foam layer have for example between 100 μm and 6000 μm, 200 μm and 4000 μm it Between, the thickness between 500 μm and 2000 μm or between 800 μm and 1500 μm.

Polymer foam layer can have in 0.45g/cm³And 1.5g/cm³Between, in 0.45g/cm³And 1.10g/cm³It Between, in 0.50g/cm³And 0.95g/cm³Between, in 0.60g/cm³And 0.95g/cm³Or in 0.70g/cm³And 0.95g/cm³It Between density.The density is realized in polymer substrate by the way that gap or hole to be mixed to foam.In general, polymer foam layer will Including by volume at least 5% and for example by volume between 15% and 45% or by volume between 20% and 45% Between gap.

Wherein the first psa layer is the sandwich layer of multilayer PSA components and the epidermis that the second psa layer is multilayer PSA components Table sheath core multilayer PSA components can advantageously comprise the sandwich layer (that is, first psa layer) for polymer foam layer.When this is configured with It is referred to as ELECTRODE WITH BILAYER POLYMERIC object foam band component.

Compared with single layer PSA, according to the multilayer PSA components of the disclosure, especially ELECTRODE WITH BILAYER POLYMERIC object foam band component can To be advantageous, because the formula that can be based on the second psa layer (commonly referred to as epidermis) adjusts adhesion characteristic, while polymerization can be passed through Object froth bed (commonly referred to as sandwich layer) is formulated to solve the needs of other characteristic/overall assembly, and such as application problem, deformation are asked Topic and Energy distribution.In some embodiments, multilayer PSA components as disclosed herein be it is smooth, homogenization and The layer combined by mutual chemical forms.

In some cases it may be beneficial to which the multilayer PSA components of the disclosure further include third psa layer, the 3rd PSA For layer in the side of the first psa layer adjacent to the first psa layer, the side is opposite with the neighbouring side of the first psa layer of second psa layer, To form three layers of multilayer PSA components.

Alternatively, the form of table sheath core/epidermis multilayer PSA components can be used in three layers of multilayer PSA components, Wherein the first psa layer is the sandwich layer of multilayer PSA components, and the first epidermis that the second psa layer is multilayer PSA components, and Third psa layer is the second epidermis of multilayer PSA components.

As expected the thickness of various psa layers and one or more of the other optional layer that PSA components include can be held Line mode and correlation properties and change in a wide range.For example, the thickness of each layer can be selected independently in 25 μm and 6000 μm Between, between 40 μm and 3000 μm, between 50 μm and 3000 μm, between 75 μm and 2000 μm or in 75 μm and 1500 μ Between m.Unless otherwise specified, it should be appreciated that all ranges in the disclosure are intended to include their endpoint.

According to specific executive mode, wherein multilayer PSA components take the form of table sheath core multilayer PSA components, wherein First psa layer is the sandwich layer of multilayer PSA components, and the epidermis that the second psa layer is multilayer PSA components, preferably second Psa layer has the lower thickness compared with the first psa layer.In the executive mode that wherein the first psa layer is polymer foam layer, This is especially beneficial, to form foam of polymers PSA tape material.For example, the thickness of the second psa layer can usually at 20 μm extremely In the range of 250 μm or 40 μm to 200 μm, and the thickness of polymer foam layer can usually 100 μm to 6000 μm, 400 μm extremely In the range of 3000 μm or 800 μm to 2000 μm.Such multilayer PSA components can express out high peel adhesion.In some cases Under, improved peel adhesion can be due to the stabilization of relatively thick polymer foam layer compared with the first psa layer.

For the ease of handling and storing, optionally at least one upper offer of the main surface of the PSA components provided Release liner.It can be used any suitable material known to technical staff as release liner, such as siliconised paper or silication polymerization Object membrane material, especially silication PET- films or silication PE or PE/PP blend membrane material.

Hollow packing

The PSA material provided includes hollow non-porous particulate filler.The non-porous particulate filler of exemplary hollow for this paper Including but not limited to it is selected from those listed below：Hollow glass microballoon, hollow inorganic bead, hollow inorganic particles, hollow titanium dioxide Silicon particle, hollow carbide particle (such as silicon-carbide particle, boron carbide particles), hollow nitride particles (such as carbonitride Grain, aluminum nitride particle, silicon nitride particle, boron nitride particle), hollow polymer particle and their mixture.

Preferred hollow non-porous particulate filler is made of inorganic material.Even further preferably, hollow non-porous particulate filler is Obturator-type particulate inorganic material.

In a specific aspect, hollow non-porous particulate filler is selected from hollow glass microballoon, hollow ceramic particle, hollow glass Ball, hollow inorganic bead and their mixture.

The hollow non-porous particulate filler for being used for this paper in a preferred aspect, is made of hollow glass microballoon.

Suitable hollow non-porous particulate filler can be commercially available from various packing material suppliers.Hollow glass for this paper Glass microballoon is for example can be with trade name 3M Glass Bubbles from the 3M companies (3M of St. Paul, MN Those of Company, St.Paul, MN) commercially available.

Suitable hollow non-porous particulate filler for this paper can have various granularities, grain shape, size distribution, particle Aspect ratio, and be not particularly limited.The selection of such parameter is depending on the specific spy needed for the first psa layer and/or PSA components Property.

Suitable hollow non-porous particulate filler can be at least 1 μm, at least 10 μm, at least 30 μm or at least 50 μm it is flat Equal granularity.In some embodiments, average particle size can be up to 500 μm, at most 300 μm, at most 200 μm, at most 150 μm, Or at most 100 μm.

Hollow non-porous particulate filler can have made of substantially spherical shape.Average particle size as described above will correspond to hollow The number average diameter of nonporous packing particle.

In an exemplary embodiment, relative to the overall weight of psa layer, the PSA that is provided include at least 5 weight %, The hollow non-porous particle of at least 6 weight %, at least 7 weight %, at least 8 weight %, at least 9 weight % or at least 10 weight % Filler.In an exemplary embodiment, relative to the overall weight of psa layer, the PSA that is provided includes at most 20 weight %, extremely More 17 weight %, at most 15 weight %, at most 14 weight %, at most 13 weight % or at most 12 weight %'s is hollow non-porous micro- Particulate filler.

It is believed that the use of the hollow non-porous particulate filler with hydrophobic surface modification in situ can be provided with beneficial to (micro- See) the PSA components of mechanical property are related to the improved stripping performance in various substrates.Hollow non-porous particulate filler is dredged Aqueous surface is modified surrounding resin matrix (the especially polymer precursor composition that can influence filler particles and the first psa layer strongly Object) between interaction.

The achievable resin Composition matrix of use and filler with the hollow non-porous particulate filler that hydrophobic surface is modified Layering between the surface of grain.It is believed that these weaker interactions between hardening resin matrix and filler particles, Yi Jiyin The improved deformability of this gained PSA component, causes through the better stress distribution/dissipation of PSA components, this is then various Improved stripping performance is provided on base type.

Hydrophobic surface, which is modified, to be obtained by being chemically treated, and in particular, by by including (methyl) acrylic acid Arrcostab, hollow non-porous particulate filler and comprising hydrophobicity alkoxy silane or hydrophobicity organofunctional polysiloxane The in-situ chemical surface functionalization that the curable precurser composition of surface modifier provides obtains.

The hydrophobic surface modification of hollow non-porous particulate filler can pass through nonpolar base with non-polar group (alkyl group) Group (preferably, alkyl group) and hollow non-porous particulate filler surface between covalent bond, and by covalent siloxanes key come It executes.

In the PSA provided, the surface of hollow non-porous particulate filler is by making hollow non-porous particulate filler change with surface Property agent occur chemical reaction and become hydrophobic.

It is highly preferred that the surface of hollow non-porous particulate filler is by making hollow non-porous particulate filler and hydrophobic silane, dredging Aqueous organofunctional polysiloxane or combination thereof or mixture occur chemical reaction and become hydrophobic.It is available Hydrophobic silane includes alkoxy silane.

Especially useful alkoxy silane and organofunctional polysiloxane has following chemical constitution：

(R¹-O)_m(R²)_pSi-[(O-Si(OR¹)_q(R²)_2-q)_x-Si(O-R¹)_m(R²)_3-m]_r,

Wherein R¹It independently is alkyl, R²Independently be hydrophobic part, selected from saturation, unsaturation, straight chain, branch and Cricoid alkyl and combination thereof, in the range of 0 to 3, in the range of 0 to 3, in the range of 0 to 2, r's q exists p m In the range of 0 to 4, x is in the range of 0 to 9, and wherein summation m+p+r is equal to 4 and there are at least one R¹At least one A R²。

As used above, term " independently " indicates R¹Or R²Each of it is specified indicate may or may not in chemical constitution Other places pass through the similar specified identical chemical group of another group indicated.

Optionally, R¹With 1 to 6 carbon atom or more preferable 1 to 4 carbon atom.R¹It can be independently selected from methyl, second Base, propyl and butyl, and it is more preferably selected from methyl and ethyl.

Optionally, m is in the range of 1 to 3, and it is 3 that m, which is 2 or 3 or m,.

Optionally, R²Can have 1 to 100 carbon atom, 1 to 50 carbon atom, 1 to 30 carbon atom or 1 to 25 carbon Atom.In some embodiments, R²Selected from methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, the last of the ten Heavenly stems Base, undecyl, dodecyl, tridecyl, myristyl, pentadecyl, cetyl, heptadecyl, octadecyl, ten Nine alkyl, eicosyl and its fluorinated derivatives, 13 fluoro- 1,2,2,2- tetrahydrochysenes octyls；More preferably, however, R²It is independent Ground is selected from methyl, propyl, n-octyl and cetyl.

In the above chemical constitution, it is noted that for alkoxy silane, r 0, and for the poly- silica of functional organic Alkane, r is in the range of 1 to 4.

Alkoxy silane and organofunctional polysiloxane generate alcohol when being reacted with such as water or siliceous material.Work as R²For When ethyl, alkoxy silane and organofunctional polysiloxane discharge alcohol ethyl alcohol.Due to coming from Environment, Health and Safety angle It says, ethyl alcohol is relative benign, therefore R²Preferably ethyl group.

The use of organofunctional polysiloxane can provide other advantage.For example, alkoxy silane and functional organic The volatility of polysiloxanes is usually reduced with the increase of molecular weight.Volatile organic compounds can be in a manufacturing environment one The fifth wheel of work is played, because they may need separation or in another way recapture.With their parent alkoxy Silane is compared, and oligomeric organofunctional polysiloxane releases volatile organic compounds in notable smaller degree.Cause This, r is preferably in the range of 1 to 4.

Advantageously, the hydrophobicity of hollow non-porous particulate filler can be carried out when filler and curable precurser composition are compounded Surface is modified.As it was noted above, this represents the notable technical advantage of manufacturing process, because in-situ-surface modifying can avoid being compounded Change processing step required when filler particles before.Other than silylation step itself, such processing step may include, example Such as, the cleaning, flushing and drying of the filler particles of surface treatment.Manufacture efficiency can be significantly improved by eliminating these steps, be dropped simultaneously Low solvent consumption and waste.

Surface modifier can provide in liquid medium, or poly- preferably as pure alkoxy silane, functional organic Siloxanes or combination thereof or mixture provide.Surface modifier can be enough to provide the hydrophobic of hollow non-porous particulate filler Property the surface amount that is modified exist, and the total weight gauge based on curable precurser composition can be at least 0.1%, at least 0.2%, 0.4%, 0.6% or at least 0.8%.In some embodiments, the overall weight based on curable precurser composition Meter, the amount of surface modifier can be up to 4%, at most 3%, at most 2%, at most 1.5% or at most 1.2%.

PSA monomers

In a specific aspect, the first psa layer and/or the second psa layer and/or third psa layer include polymeric matrix material Material, the polymeric matrix material are selected from polyacrylate, polymethacrylates, polyurethane, polyolefin, polyamine, polyamide, gather Ester, polyethers, polyisobutene, polystyrene, polyethylene, polyvinylpyrrolidone, natural rubber and synthetic rubber and they Copolymer and blend.

Preferably, the PSA provided include polymeric matrix material, the polymeric matrix material be selected from polyacrylate, Polymethacrylates and polyurethane and their copolymer and blend.It is highly preferred that the first psa layer and/or second Psa layer and/or third psa layer include polyacrylate.

It is preferred that poly- (methyl) acrylate can by including linear chain or branched chain (methyl) alkyl acrylate, preferably have comprising It is preferred that the nonpolarity of the linear or branched alkyl group group of 1 to 32 carbon atom, 1 to 20 carbon atom or 1 to 15 carbon atom is straight The monomer component of chain or branch (methyl) alkyl acrylate is polymerized.

Herein, term " (methyl) alkyl acrylate (alkyl (meth) acrylate) " and " (methyl) acrylic acid alkyl Ester (alkyl (meth) acrylate ester) " is used interchangeably.Term " (methyl) acrylate " refers to acrylate, methyl Acrylate, or both.Term " (methyl) acrylic acid " be methacrylic acid, acrylic acid, or both." it is based on (methyl) third The material of olefin(e) acid " refers to by one or more materials that there is the monomer of (methyl) acryloyl group to prepare, (methyl) third Enoyl- group is by formula CH₂The group that=C (R)-(CO)-is indicated, wherein R are hydrogen or methyl.

Term " alkyl " refers to the univalent perssad for saturated hydrocarbons.Alkyl can be straight chain, branch, it is cricoid or they Combination, and usually there is 1 to 32 carbon atom.Given alkyl group can contain 1 to 25 carbon atom, 1 to 20 carbon atom, 1 to 18 carbon atom, 1 to 12 carbon atom, 1 to 10 carbon atom, 1 to 8 carbon atom, 1 to 6 carbon atom or 1 to 4 Carbon atom.The example of alkyl group includes but not limited to methyl, ethyl, n-propyl, isopropyl, normal-butyl, isobutyl group, tertiary fourth Base, n-pentyl, n-hexyl, cyclohexyl, n-heptyl, n-octyl, 2- ethylhexyls, 2- octyls and 2- propylheptyls.

Term " glass transition temperature " and " T_g" it is used interchangeably and refers to the glass transition of material or mixture Temperature.Unless otherwise specified, glass transition temperature is measured by differential scanning calorimetry.

Available (methyl) alkyl acrylate includes：(methyl) methyl acrylate, (methyl) ethyl acrylate, (methyl) acrylic acid n-propyl ester, (methyl) isopropyl ester, n-butylacrylate, isobutyl acrylate, (first Base) acrylate tert-buthyl, (methyl) acrylic acid n-pentyl ester, (methyl) acrylic acid isoamyl base ester, (methyl) acrylic acid just oneself Base ester, (methyl) acrylic acid dissident base ester, (methyl) cyclohexyl acrylate, (methyl) phenyl acrylate, (methyl) propylene Misery base ester, (methyl) iso-octyl acrylate, (methyl) acrylic acid 2- octyls ester, (methyl) 2-ethylhexyl acrylate, (methyl) decyl acrylate, (methyl) lauryl acrylate, (methyl) acrylic acid 2- propylheptyls ester, (methyl) acrylic acid Stearyl base ester, isobornyl acrylate, (methyl) benzyl acrylate ester, octadecyl acrylate, nonylphenol acrylate Ester, dodecylacrylate, the different Fo Er esters of (methyl) acrylic acid (isophoryl (meth) acrylate) and their group Conjunction or blend.

(methyl) alkyl acrylate of preferred linear chain or branched chain includes (methyl) Isooctyl acrylate monomer, (methyl) propylene Sour 2- ethylhexyls, (methyl) acrylic acid 2- Propylheptyls, (methyl) acrylic acid 2- monooctyl esters, butyl acrylate cores and they Combination or mixture.Especially preferred (methyl) alkyl acrylate include Isooctyl acrylate monomer, 2-EHA, Acrylic acid 2- monooctyl esters and acrylic acid 2- Propylheptyls.

In an exemplary embodiment, (methyl) alkyl acrylate of linear chain or branched chain is (methyl) acrylic acid 2- Monooctyl ester.When in the curable precurser composition provided in use, such as with other isomers of (methyl) 2-ethyl hexyl acrylate N-octyl is compared with different monooctyl ester, and (methyl) acrylic acid 2- monooctyl esters provide comparable adhesion characteristic.Advantageously, when with derived from other When the adhesive composition of octyl isomers (such as Isooctyl acrylate monomer) is compared, under same concentrations and in same polymeric item Under part, such curable precurser composition can have lower intrinsic viscosity and solution viscosity.

(methyl) third can be prepared by sec-n-octyl alcohol and (methyl) Diacryloyl derivative such as ester, acid and halogen acyl by routine techniques Olefin(e) acid 2- monooctyl esters.Sec-n-octyl alcohol can by with naoh treatment be derived from castor oil ricinoleic acid (or its ester or halogen acyl), later It is distilled out from by-product decanedioic acid and is prepared.

Polymer used herein based on (methyl) acrylic acid is usually by having opposite lower glass transition temperatures (T_g) (that is, the T of monomer_gMeasured by the homopolymer prepared by monomer) one or more nonpolar acrylate monomers plus each The optional such as one or more polar monomers of monomer are planted to prepare.Polar monomer can have acidic-group, hydroxyl group or contain Nitrogen groups.

Nonpolar acrylate monomer in the conventional elastomeric material based on (methyl) acrylic acid includes acrylic acid 2- second The own ester of base (2-EHA) and Isooctyl acrylate monomer (IOA).

In some embodiments, polymeric matrix material further includes polar comonomers.Comonomer can be, for example, Polar acrylate.Preferred comonomer includes acrylic acid, methacrylic acid, itaconic acid, acrylic acid hydroxy alkyl ester, acryloyl Amine (acrylamide) and substitution acrylamide, acrylamide (acrylamine) and replace acrylamide and they Combination and mixture.Other polar comonomers include acrylamide, acrylonitrile, methacrylonitrile, the acrylic acid of n- substitutions Hydroxy alkyl ester, acrylic acid cyanoethyl ester, maleic anhydride, n- vinyl-2-pyrrolidones, n- vinyl-caprolactam and it Combination or mixture.

In an exemplary embodiment, for the first psa layer of PSA components and/or the second psa layer and/or third psa layer Including PSA composition, the PSA composition includes the reaction product of curable precurser composition, the curable precurser combination Object includes：

(a) as the linear chain or branched chain of principal monomer (methyl) alkyl acrylate, principal monomer is preferably selected from (methyl) Isooctyl acrylate monomer, (methyl) 2-EHA, (methyl) acrylic acid 2- Propylheptyls, butyl acrylate；And

(b) optionally, the second comonomer with ethylenically unsaturated group, it is preferably copolymerizable with acrylate principal monomer Enhance Mono-olefinic unsaturated monomer.

In some illustrative aspects, the first psa layer and/or the second psa layer for generating PSA components and/or the 3rd PSA The curable precurser composition of layer includes at least one second comonomer with ethylenically unsaturated group.It is any suitable that there is alkene Belong to unsaturated group second comonomer can be adopted to prepare the first psa layer for generating PSA components and/or the second psa layer and/ Or the curable precurser composition of third psa layer.According to present embodiment, those skilled in the art are by easy knowledge Not Yong Yu this paper the suitable second comonomer with ethylenically unsaturated group.

The illustrative second comonomer with ethylenically unsaturated group includes being selected from those listed below：Polarity and nonpolarity (methyl) alkyl acrylate, polar monomer and non-polar vinyl monomers and combination thereof and mixture.

In one embodiment, the second comonomer with ethylenically unsaturated group includes (methyl) alkyl acrylate, It is preferred that with the alkyl group for including 1 to 32 carbon atom, 1 to 20 carbon atom or 1 to 15 carbon atom.

Curable precurser composition may also include the second non-polar monomer with ethylenically unsaturated group.Not with olefinic Any non-polar monomer of saturated group is used as being used to prepare the first psa layer and/or second for generating PSA components The second comonomer of the curable precurser composition of psa layer and/or third psa layer.There is ethylenically unsaturated group for this paper Suitable non-polar monomer be as known in the art.

Suitable the second non-polar monomer with ethylenically unsaturated group includes but not limited to nonpolar (methyl) propylene Acid alkyl ester.In particular, second comonomer includes 1 to 32 carbon atom, 1 to 20 carbon atom, 1 to 15 carbon original including having Nonpolarity (methyl) alkyl acrylate of the alkyl group of son or 1 to 13 carbon atom.

For this paper include with 1 to 30 carbon atom alkyl group nonpolarity (methyl) alkyl acrylate packet It is different to include but be not limited to (methyl) methyl acrylate, (methyl) ethyl acrylate, (methyl) n-propyl, (methyl) acrylic acid Propyl ester, (methyl) n-butyl acrylate, (methyl) isobutyl acrylate, (methyl) tert-butyl acrylate, (methyl) acrylic acid are just Pentyl ester, (methyl) isoamyl acrylate (iso-pentyl (meth) acrylate) are (that is, (methyl) isoamyl acrylate (iso- Amyl (meth) acrylate)), (methyl) acrylic acid 3- pentyl esters, (methyl) acrylic acid 2-methyl-1-butene ester, (methyl) propylene Sour 3- methyl-1s-butyl ester, (methyl) stearyl acrylate, (methyl) phenyl acrylate, (methyl) the just own ester of acrylic acid, (methyl) Isohexyl acrylate, (methyl) cyclohexyl acrylate, (methyl) acrylic acid 2- methyl-1-pentenes ester, (methyl) acrylic acid 3- methyl- 1- pentyl esters, (methyl) acrylic acid 4- methyl -2- pentyl esters, (methyl) acrylic acid 2- ethyl -1- butyl esters, (methyl) acrylic acid 2- first The own esters of base -1-, the own esters of (methyl) acrylic acid 3,5,5- triethyl groups -1-, (methyl) cyclohexyl acrylate, (methyl) acrylic acid 3- heptan Ester, (methyl) benzyl acrylate, (methyl) n-octyl, (methyl) Isooctyl acrylate monomer, (methyl) acrylic acid 2- are pungent Ester, the own esters of (methyl) acrylic acid 2- ethyls -1-, the positive last of the ten Heavenly stems ester of (methyl) acrylic acid, (methyl) isodecyl acrylate, (methyl) propylene Sour isobornyl thiocyanoacetate, (methyl) acrylic acid 2- Propylheptyls, the different nonyl ester of (methyl) acrylic acid, the different Fo Er esters of (methyl) acrylic acid (isophoryl (meth) acrylate), (methyl) acrylic acid n-dodecane base ester (that is, (methyl) lauryl acrylate), (first Base) acrylic acid n-tridecane base ester, (methyl) acrylic acid isotridecyl ester, (methyl) acrylic acid 3,7- dimethyl-monooctyl ester, with And any combination of them or mixture.

Other suitable (methyl) alkyl acrylates include having containing at least 14 carbon atoms but for straight chain or having Those of the alkyl group of single branch point.Example includes but not limited to (methyl) acrylic acid 1- stearyls, (methyl) third Olefin(e) acid 17- methyl-1s-heptadecane base ester and (methyl) acrylic acid 1- tetradecane base esters.

Other suitable nonpolar (methyl) acrylate for this paper are (methyl) benzyl acrylate, such as (first Base) phenyl acrylate or (methyl) benzyl acrylate；(methyl) acrylic acid alkenyl esters, such as (methyl) acrylic acid 3, 7- dimethyl -6- octene-1s-base ester and (methyl) allyl acrylate；And (methyl) acrylic acid alkyl of aryl substitution Ester or (methyl) alkyl acrylate of aryloxy group substitution, such as (methyl) acrylic acid 2- biphenyl hexyl ester, (methyl) third Olefin(e) acid benzyl ester and (methyl) acrylic acid 2- phenoxyethyl acrylates.

When being shaped to homopolymer (that is, the polymer prepared using the monomer of single type), the second nonpolarity in PSA Monomer has relatively high T_gCan be advantageous, because these monomers have the T for adjusting curable precurser composition_gIn order to provide The ability of the adhesive strength of enhancing.When being shaped to homopolymer, these monomers can have at least 20 DEG C or at least 25 DEG C or extremely Few 30 DEG C or at least 40 DEG C or at least 50 DEG C of glass transition temperature (T_g).Alternatively, when being shaped to homopolymer, PSA In the second non-polar monomer can also have relatively low T_g- for example, being less than 20 DEG C of T_g。

The second comonomer with ethylenically unsaturated group for this paper may include with acidic-group and single olefinic not The monomer (that is, acid monomer) of saturated group.These monomers are typically polarity or highly polar.Polarity (or hydrogen bonding capability) is normal Often by use such as " strong ", " in " and the term of " weak " be described.The reference text of these and other solubility term is described It offers including Solvents (solvent), (Paint Testing Manual, 3rd ed., G.G.Seward, Ed., American (U.S. for being located at Pennsylvania Philadelphia tries by Society for Testing and Materials, Philadelphia, PA It tests and materials association《Paint manual testing》3rd edition, G.G.Seward is edited)) and A Three-Dimensional Approach to Solubility (three-dimensional method of solubility), Journal of Paint Technology (paint technologies Magazine), volume 38, No. 496, the 269-280 pages.Ethylenically unsaturated group can be (methyl) acryl group or not be The vinyl groups of (methyl) acryl group is (that is, CH₂=CH₂Group).Illustrative acid monomer can have carboxylic acid group, Sulfonic group, phosphonic acid base or their salt.Due to its availability, so usually acid of the selection with carboxylic acid group or their salt Property monomer.If necessary to stronger acidic-group, the monomer with phosphonic acid base, sulfonic group or their salt may be used.It is acid The example of monomer includes but not limited to, (methyl) acrylic acid, itaconic acid, fumaric acid, crotonic acid, citraconic acid, maleic acid, oleic acid, (methyl) β-acryloxypropionic acid, methacrylic acid 2- sulfoethyls ester, styrene sulfonic acid, 2- acrylamido -2- methyl-prop sulphurs Acid, vinyl phosphonic acid or their mixture.The salt of any suitable acidic-group can be used.In many embodiments, salt Cation be alkali metal ion (such as sodium, potassium or lithium ion), alkaline-earth metal ions (such as calcium, magnesium or strontium ion), ammonium from Son or the ammonium ion replaced by one or more alkyl or aryl groups.

Highly polar monomer includes acrylic acid, methacrylic acid, itaconic acid, acrylic acid hydroxy alkyl ester, acrylamide and substitution Acrylamide, and such as n- vinyl pyrrolidones, n- caprolactams, acrylonitrile, vinyl chloride, phthalic acid two Allyl ester and the typical case that (methyl) acrylic acid n, n- dialkyl amino base ester is moderately polar monomer.Polar monomer it is another Outer example includes acrylic acid cyano ester, fumaric acid, crotonic acid, citric acid, maleic acid, β-acryloxypropionic acid or metering system Sour sulphur ethyl ester.As above (methyl) alkyl acrylate monomer enumerated is the typical case of relatively weak polar monomer.These Example was provided and is understood not to restrictive for the reasons why illustrating.In the polarity list as second comonomer In the group of body, acrylic acid and n- caprolactams are particularly preferred.

When PSA components are intended to be bonded to LSE substrates, the curable precurser of one or more psa layers of multilayer PSA components Composition may include the total weight based on curable precurser composition, the at most highly polar acrylate or 0.1 of 10 weight % Weight % to 10 weight %, 0.5 weight % are to 10 weight %, 1.0 weight % to 10 weight %, 2.0 weight % to 8.0 weights Measure %, 2.5 weight % to 6.0 weight % or 3.0 weight % to 6.0 weight %.

Second comonomer with ethylenically unsaturated group may include having single ethylenically unsaturated group and hydroxyl group Those.Ethylenically unsaturated group can be (methyl) acryl group or vinyl groups (i.e. CH₂=CH₂Group).With hydroxyl The exemplary monomer of base group includes but not limited to, (methyl) acrylic acid hydroxy alkyl ester (for example, 2-Hydroxy ethyl acrylate or Acrylic acid -3- hydroxy propyl esters), hydroxyalkyl (methyl) acrylamide is (for example, 2- hydroxyethyl acrylamides or 3- hydroxypropyl acryloyls Amine) and ethoxylation hydroxyethyl methacrylate (for example, can be with trade name CD570, CD571, CD572 from guest's sunset method Ni Zhou The commercially available monomer of the Sartomer (Sartomer) of Exton (Exton, PA)).

Second comonomer with ethylenically unsaturated group further include have single ethylenically unsaturated group and nitrogen-containing group or Those of their salt.Ethylenically unsaturated group can be (methyl) acryl group or vinyl groups (i.e. CH₂=CH₂Base Group).The example of nitrogen-containing group includes but not limited to secondary acylamino- and tertiary acylamino-.The illustratively polarity list with secondary acylamino- Body includes but not limited to n- alkyl (methyl) acrylamide, such as n- Methacrylamides, n- ethyl acrylamides, n- isopropyls third Acrylamide, t-octyl acrylamide or n- octyl acrylamides.Illustratively the polar monomer with tertiary amido groups includes But it is not limited to n- caprolactams, n- vinyl-2-pyrrolidones, acryloyl morpholine and n, n- dialkyl acrylamides Amine, such as n, n- dimethacrylamide, n, n- acrylamides, n, n- dipropyl acrylamide and n, n- dibutyl Acrylamide and combination thereof and mixture.

Polarity second comonomer with ethylenically unsaturated group further includes having single ethylenically unsaturated group and ether (that is, the group of alkylidene-oxygen-alkylidene comprising at least one formula-R-O-R-, wherein each R is with 1 to 4 carbon atom Alkylidene) those of.Including but not limited to alkoxylated (methyl) alkyl acrylate of illustrative monomer, such as propylene Acid card must ester, acrylic acid -2- methoxy acrylates and acrylic acid -2- ethoxy ethyl esters；And poly- (alkylene oxide) acrylate, such as Poly- (ethylene oxide) acrylate and poly- (propylene oxide) acrylate.Sometimes referred to as poly- (the alkylene of poly- (alkylene oxide) acrylate Glycol) acrylate.These monomers can have any suitable end group, such as hydroxyl group or alkoxy base.For example, when end When base is methoxyl group, monomer can be described as methoxyl group poly(ethylene glycol) acrylate.

Polar monomer can be added, to increase one or more psa layers of PSA components to adjacent layer such as substrate or back sheet Bonding force, enhance the cohesive strength of PSA, or both.In some illustrative aspects, based on for generating the specific of PSA components The amount of the total weight of the curable precurser composition of pressure sensitive adhesive layer, polar monomer is at most 15 weight %.One In the case of a little, the amount of polar monomer can 0.1 to 15 weight % of the first polar monomer, 0.5 to 15 weight %, 1.0 to In the range of 10 weight %, 2.0 to 8.0 weight %, 2.5 to the 6.0 weight weight of % or 3.0 to 6.0 %.Other show at some In terms of example property, which is usually at most 10 weight % or at most 5 weight %.For example, based on the specific pressure for generating PSA components The total weight of the curable precurser composition of sensitive adhesive layer, the amount of polar monomer can 0 to 15 weight %, 0.5 to 15 weight %, 1 to 15 weight %, 0 to 10 weight %, 0.5 to 10 weight %, 1 to 10 weight %, 0 to 5 weight %, 0.5 to 5 In the range of the weight weight of % or 1 to 5 %.

In some embodiments, the total weight based on curable precurser composition, curable precurser composition include At least (methyl) alkyl acrylate of the linear chain or branched chain of 50 weight % is as principal monomer and at most 15 weight % or extremely The polar monomer of more 10 weight %, preferably polar acrylate.

In some embodiments, the total weight based on curable precurser composition, curable precurser composition include The polarity list of at least 0.1 weight %, at least 0.5 weight %, at least 1 weight % or at least 2 weight % or at least 3 weight % Body, preferably polar acrylate.

In some embodiments, the curable precurser composition for generating PSA includes：A) 50 to 99.5 weight %, Or 60 to 90 weight % linear chain or branched chain (methyl) alkyl acrylate as its principal monomer, wherein principal monomer is preferred Selected from (methyl) Isooctyl acrylate monomer, (methyl) 2-EHA, (methyl) acrylic acid 2- Propylheptyls, acrylic acid fourth Ester or their mixture；B) 0 to 50 weight %, 3 to 40 weight %, 5 to the 35 weight weight of % or 10 to 30 % have The second comonomer of ethylenically unsaturated group, preferably the second non-polar monomer with ethylenically unsaturated group；C) 0 to 15 weight The polar monomer of %, 0.5 to 15 weight %, 1 to 10 weight %, 2 to 8 weight %, 2 to the 6 weight weight of % or 3 to 6 % are measured, It is preferred that polar acrylate；And d) optionally, tackifying resin, wherein all wt percentage are based on curable precurser combination The total weight of object.

In some embodiments, the curable precurser composition for generating PSA includes：A) as the straight of principal monomer Chain or branch (methyl) alkyl acrylate, wherein principal monomer are preferably selected from (methyl) Isooctyl acrylate monomer, (methyl) propylene Sour 2- ethylhexyls, (methyl) acrylic acid 2- Propylheptyls, butyl acrylate；B) 0 to 50 weight %, 3 to 40 weight %, 5 to The second comonomer with ethylenically unsaturated group of the 35 weight weight of % or 10 to 30 % preferably has ethylenically unsaturated group The second non-polar monomer；C) 0 to 15 weight %, 0.5 to 15 weight %, 1 to 10 weight %, 2 to 8 weight %, 2.5 to 6 weights Measure the first polar monomer of the weight of % or 3 to 6 %, preferably polar acrylate；D) optionally, the second polar monomer, preferably pole Property non-acrylate monomers；And e) optionally, tackifying resin；Wherein all wt percentage is based on curable precurser combination The total weight of object.

Optionally, curable precurser composition further includes one or more other vinyl monomers, such as vinyl esters (example Such as, vinyl acetate and vinyl propionate)；Styrene or their derivative, such as alkyl-substituted styrene is (for example, α- Methyl styrene)；Vinyl halide；Or mixtures thereof.Such monomer can be polarity or nonpolar.If it does, these Vinyl monomer can any suitable amount presence.In some embodiments, the total weight based on curable precurser composition Meter, vinyl monomer exist with the amount of at most 5 parts by weight.For example, vinyl monomer can be at most 4 weight %, at most 3 weights The amount for measuring % or at most 2 weight % uses.In some embodiments, the amount of vinyl monomer 0 to 5 weight %, In the range of 0.5 to 5 weight %, 1 to 5 weight %, 0 to the 3 weight weight of % or 1 to 3 %.

Tackifier

Curable precurser composition may also include tackifier (also referred to as tackifying resin), and amount is usually curable precurser group Close 2 to 30 weight %, 4 to the 20 weight weight of % or 6 to 12 % of object.

It optionally, can be by one or more tackifier, one or more plasticizer or their mixture and before can be cured Body combination of compositions.Tackifier and plasticizer are advantageously used for adjusting the T of PSA_g, storage modulus and adherence.

Be included in any tackifier in curable precurser composition preferably with other groups in curable precurser composition Divide miscible.Any tackifier being typically included in conventional PSA composition can be used.Solid or liquid tackifiers can be added. Solid tackifier usually has 10,000g/mol or smaller weight average molecular weight (or M_w) and about 70 DEG C or more of softening point.Liquid Body tackifier are the cohesive material with about 0 DEG C to about 70 DEG C of softening point.

Tackifier include rosin resin, such as the derivative (for example, rosin ester) of rosin acid and they；Terpene resin is such as Polyterpene (for example, the resin based on australene, the resin based on nopinene, and resin based on limonene) and aromatic modified polyterpene Resin (for example, phenol-modified polyterpene resin)；Coumarone-indene resin and hydrocarbon resin based on oil, such as based on C5's Hydrocarbon resin, the hydrocarbon resin based on C9, the hydrocarbon resin based on C5/C9 and the resin based on bicyclopentadiene.It, can if be added Tackifying resin is hydrogenated, the color of specific pressure-sensitive adhesive composition is contributed with reducing them.If desired, can be used various The combination of tackifier.

Rosin ester tackifier is the reaction product of various rosin acids and alcohol.These include but not limited to the methyl of rosin acid The pentaerythritol ester of ester, the triglycol ester of rosin acid, the glyceride of rosin acid and rosin acid.These rosin esters can part Or it is completely hydrogenated, to improve stability and reduce their Color influences to pressure-sensitive adhesive composition.Rosin resin tackifier It can be for example with trade name PERMALYN, STAYBELITE and FORAL from Eastman Chemical Company (Eastman Chemical Company) commercially available, and with trade name NUROZ and NUTAC from New Port industrial group (Newport Industries) quotient Purchase obtains.Completely hydrogenated rosin resin can be for example with trade name FORAL AX-E from Eastman Chemical Company (Eastman Chemical Company) it is commercially available.Partially hydrogenated rosin resin can be for example with trade name STAYBELITE-E from her scholar Graceful chemical company is commercially available.

Tackifier based on hydrocarbon resin can be prepared by the various raw materials based on oil.These raw materials can be that aliphatic hydrocarbon is (main For C5 monomers, and there are some other monomers, such as anti-form-1,3- pentadienes, cis- -1,3-pentadiene, 2- methyl -2- fourths The mixture of alkene, bicyclopentadiene, cyclopentadiene and cyclopentene), aromatic hydrocarbon (predominantly C9 monomers, and that there are some is other The mixture of monomer, such as vinyltoluene, bicyclopentadiene, indenes, methyl styrene, styrene and methyl indenes) or they Mixture.Tackifier derived from C5 monomers are referred to as the hydrocarbon resin based on C5, and are referred to as base derived from those of C9 monomers In the hydrocarbon resin of C9.Some tackifier be derived from C5 and C9 monomers mixture, or for based on C5 hydrocarbon tackifier and be based on The blend of the hydrocarbon tackifier of C9.In these resins it is any can partly or completely perhydrogenating with improve they color, they Thermal stability or their processing compatibility.

Hydrocarbon resin based on C5 can be with trade name PICCOTAC and EASTOTAC from this golden baud of Tennessee State The Eastman Chemical of (Kingsport, TN), with trade name WINGTACK from the Cray prestige of Pennsylvania's Exton Sharp company (Cray Valley, Exton, PA), with trade name NEVTAC LX from the Nevilleization of Pittsburgh of Pennsylvania Company (Neville Chemical Company, Pittsburgh, PA), and with trade name HIKOREZ from Korea S Guo Chuan The Cologne industrial group (Kolon Industries, Inc., Gwacheon, South Korea) in city is commercially available.Various hydrogenations The C5 bases hydrocarbon resin of degree can be commercially available from Eastman Chemical Company with trade name EASTOTACK.

Hydrocarbon resin based on C9 can with trade name PICCO, KRISTLEX, PLASTOLYN, PICCOTAC and ENDEX from she Shi Man chemical companies (Eastman Chemical Company) are commercially available, public from Cray Willie with trade name NORSOLENE Department (Cray Valley) is commercially available, and with trade name NOVAREZ, from Johanna Lüttge, this company (Ruetgers N.V.) is commercially available, And with trade name HIKOTAC from can grand industrial group (Kolon Industries, Inc.) it is commercially available.These resins can quilt Partially or even wholly hydrogenate.Before the hydrogenation, the C9 bases hydrocarbon resin usually aromatic substance with about 40 percentages, such as passes through proton Nuclear magnetic resonance measures.The C9 bases hydrocarbon resin of hydrogenation can be for example with trade name REGALITE and REGALREZ from eastman chemical (Eastman Chemical) is commercially available, be 50 to 100 percentages (for example, 50 percentages, 70 percentages, 90 percentages With 100 percentages) hydrogenation.The resin partly hydrogenated usually has some aromatic rings.

The various hydrocarbon tackifier based on C5/C9 can be obtained with trade name ARKON commercially available from Huang Chuan Co., Ltd. (Arakawa) , it is commercially available from Ji Weng Co., Ltd. (Zeon) with trade name QUINTONE, with trade name ESCOREZ from Texas Europe The Exxon Mobil Corporation (Exxon Mobile Corp., Irving, TX) of text is commercially available, and with trade name NURES and The Niu Bute trade Co., Ltds (Newport Industries, Surrey, UK) of H-REZ from Surrey are commercially available.

Any tackifier can be used with the amount of the at most 30 weight % of curable precurser composition.The dosage of tackifier can be At most 25 weight %, at most 20 weight %, at most 15 weight % or at most 12 weight %.The amount of tackifier can for example consolidated Change precursor composition 2 to 30 weight % in the range of, in the range of 3 to 25 weight %, in the range of 4 to 20 weight % It is interior, in the range of 5 to 15 weight % or in the range of 6 to 12 weight %.

Plasticizer

Available curable precurser composition may include one or more plasticizer.Plasticizer is for reducing composition T_g, and preferably in composition (such as curable precurser composition) other components and any optional tackifier it is compatible (i.e. miscible).Suitable plasticizer includes but not limited to, various polyalkylene oxides (such as polyethylene oxide or epoxy third Alkane), adipate ester, formic acid esters, phosphate, benzoic ether, phthalic acid ester and sulfonamide or naphthenic oil.

Crosslinking agent

Curable precurser composition also may include crosslinking agent (crosslinker) (also referred to as crosslinking agent (crosslinking agent))。

Crosslinking agent can be considered to have the second comonomer of ethylenically unsaturated group.Advantageously, crosslinking agent can significantly increase The cohesive strength and tensile strength of there is provided PSA are provided.Crosslinking agent usually has can be with the first monomer or another monomer covalent At least two functional groups of bonding.That is, crosslinking agent can have at least two ethylenically unsaturated groups.Suitable crosslinking agent usually has There are multiple (methyl) acryl groups.Alternatively, crosslinking agent can have at least two groups, these groups can be with another list Various functional groups (that is, not being the functional group of ethylenically unsaturated groups) reaction on body.For example, crosslinking agent can have multiple bases Group, these groups can be reacted with such as acidic-group of the functional group on other monomers.

Crosslinking agent with multiple (methyl) acryl groups includes two (methyl) acrylate, three (methyl) acrylic acid Ester, four (methyl) acrylate and five (methyl) acrylate.These crosslinking agents can for example by make (methyl) acrylic acid with Polyalcohol (i.e. the alcohol at least two hydroxyl groups) is reacted and is formed.There are two polyalcohol usually tools, three, four or five A hydroxyl group.The mixture of crosslinking agent can also be used.

Optionally, crosslinking agent includes at least two (methyl) acryl groups.There are two acryl group to show for tool Example property crosslinking agent includes but not limited to diacrylate 1,2- glycol esters, diacrylate 1,3-PD ester, diacrylate 1,9- Nonanediol ester, diacrylate 1,12- dodecanediols ester, diacrylate 1,4- butanediol esters, diacrylate 1,6-HD ester, Butanediol diacrylate, bisphenol a diacrylate, diethyleneglycol diacrylate, diacrylate triglycol ester, two propylene Sour tetraethylene glycol ester, diacrylate tripropylene glycol ester, polyethyleneglycol diacrylate, polypropyleneglycol diacrylate, polyethylene/ Polypropylene copolymer diacrylate, polybutadiene two (methyl) acrylate, propenoxylated three (methyl) propylene acid glycerol Ester and the ester modified caprolactone of neopentyl glycol hydroxyl peopentyl ester diacrylate.

There are three tools or the crosslinking agent of four (methyl) acryl groups includes but not limited to trimethylolpropane tris third Olefin(e) acid ester (such as can with trade name TMPTA-N from the Qing Te industrial groups of Georgia State Shi Maina (Cytec Industries, Inc., Smyrna, GA) it is commercially available and commercially available from Sartomer with trade name SR-351), three acrylic acid of pentaerythrite Ester (such as can be commercially available from Sartomer with trade name SR-444), three (2- hydroxyethylisocyanurates) triacrylates (can be commercially available from Sartomer with trade name SR-368), pentaerythritol triacrylate and pentaerythritol tetraacrylate Mixture (for example, can (ratio of wherein tetraacrylate and triacrylate be about 1 with trade name PETIA:And quotient 1) (ratio of wherein tetraacrylate and triacrylate is about 3 to name of an article PETA-K:1) commercially available from Qing Te industrial groups), Pentaerythritol tetraacrylate (such as can be commercially available from Sartomer with trade name SR-295), two-trimethylolpropanes Tetraacrylate (such as can be commercially available from Sartomer with trade name SR-355) and the pentaerythrite four of ethoxylation Acrylate (such as can be commercially available from Sartomer with trade name SR-494).There are five (methyl) acryl groups for tool Exemplary cross linking agents include but not limited to：Double pentaerythritol C5 methacrylate is (for example, public from Sartomer with trade name SR-399 It takes charge of commercially available).

In some embodiments, crosslinking agent is polymerization and includes at least two (methyl) acryl groups.Example Such as, crosslinking agent can be that poly- (alkylene oxide) at least two acryl groups (such as can be commercially available from Sartomer Polyethyleneglycol diacrylate, such as SR210, SR252 and SR603) or have at least two (methyl) acryl groups Poly- (urethane) (such as urethane diacrylate obtained from Sartomer, such as CN9018).With cross-linker molecules amount Increase, gained acrylic copolymer tend to before breaking have higher elongation.

Other types of crosslinking agent is available.Crosslinking agent, for example, can have multiple groups, these groups can be with it Functional group's such as acidic-group on its second comonomer reacts.Can be used with multiple '-aziridino groups monomer, wherein this Class monomer is reacted with carboxylic group.For example, crosslinking agent can be Bisamide crosslinker, such as 6,777,079 (Zhou etc. of United States Patent (USP) People) described in.

Crosslinking can be activated or promoted by actinic radiation (such as ultraviolet light or visible light).In these cases, can add Add photocrosslinking agent (such as UV photocrosslinking agents).These photocrosslinking agents can be used to form elastomeric material various monomers (such as Copolymerizable benzophenone) copolymerization, or can add after polymerisation.The suitable photocrosslinking agent packet added after polymerisation It includes, for example, polyfunctional benzophenone and triazine (such as XL-330, for 2,4 derived from 3M companies,-bis- (trichloromethyl) -6- (4- methoxyphenyls)-triazine).

In some embodiments, thermal cross-linking agent can be used.Optionally, thermal cross-linking agent can be with accelerating agent or flame retardant combination It uses.Suitable thermal cross-linking agent for this paper includes but not limited to isocyanates, more specifically the isocyanates of trimerization and/or The isocyanates or epoxide compound of steric hindrance without sealer, such as epoxide-amine cross linker system.Favorably Cross linker system and method be described in, for example, European patent publication EP 2305389 (Prenzel et al.), EP 2414143 (Czerwonatis et al.), EP 2192148 (Prenzel et al.), EP 2186869 (Grittner et al.), EP 0752435 (Burmeister et al.), EP1802722 (Zoellner et al.), EP 1791921 (Zoellner et al.), EP 1791922 In (Zoellner et al.) and EP 1978069 (Zoellner et al.).Suitable accelerating agent and fire retardant for this paper System is described in such as U.S. Patent number 9,200,129 (Czerwonatis et al.).Thermal cross-linking agent includes that epoxycyclohexyl spreads out Biology, specifically epoxycyclohexylcarboxylate's derivative, wherein particularly preferably (3,4- 7-oxa-bicyclo[4.1.0) methyl 3,4- epoxies Cyclohexane carboxylic acid ester, can be with trade name UVACURE 1500 from Qing Te industrial groups (Cytec Industries Inc.) quotient Purchase obtains.

If it is present crosslinking agent can any suitable amount use.In some respects, the amount of crosslinking agent is at most 5 weight %, at most 4 weight %, at most 3 weight %, at most 2 weight % or at most 1 weight %.Crosslinking agent can be for example, at least The amount of 0.01 weight %, at least 0.03 weight %, at least 0.05 weight %, at least 0.07 weight % or at least 0.09 weight % In the presence of.In some respects, the amount of crosslinking agent is in 0 to 5 weight %, 0.01 to 5 weight %, 0.05 to 5 weight %, 0 to 3 weight Measure the model of %, 0.01 to 3 weight %, 0.05 to 3 weight %, 0 to 1 weight %, 0.01 to the 1 weight weight of % or 0.05 to 1 % In enclosing.

Other than temperature-sensitive, moisture-sensitive or photosensitive crosslinker, high-energy electromagnetic radiation (such as γ or electron beam also can be used Radiation) realize crosslinking.

Initiator

Usually initiator addition is used to form in the various monomers of curable precurser composition.Polymerization initiator can be heat Initiator, photoinitiator or both.Can be used become known for Raolical polymerizable any suitable thermal initiator or Photoinitiator.Based on the total weight of curable precurser composition, the amount of initiator is usually in 0.01 weight % to 5 weights Measure % in the range of in the range of 0.01 weight % to 2 weight %, in the range of 0.01 weight % to 1 weight % or In the range of 0.01 weight % to 0.5 weight %.

In some embodiments, using thermal initiator.According to specific polymerization used, thermal initiator can be water solubility Or (that is, oil-soluble) of water-insoluble.Suitable water soluble starter includes but not limited to persulfate such as persulfuric acid Potassium, ammonium persulfate, sodium peroxydisulfate and their mixture；Oxidation-reduction initiator such as persulfate and reducing agent it is anti- Product is answered, the reducing agent such as metabisulfite (for example, sodium metabisulfite) or disulfate are (for example, hydrogen sulfate Sodium)；Or 4,4 '-azos bis- (4- cyanopentanoic acids) and its soluble-salt (for example, sodium salt, sylvite).Suitable oil-soluble initiator Including but not limited to, various azo-compounds such as can be with trade name VAZO from the E.I. E.I.Du Pont Company of Wilmington, DE Co., Ltd (E.I.DuPont de Nemours Co., Wilmington, DE) is those of commercially available, including VAZO 67 (((it is 2,2 '-for 2,2 '-azos bis- (isobutyronitriles) and VAZO 52 for 2,2 '-azos bis- (2- methylbutyronitriles), VAZO 64 Azo is bis- (2,4- methyl pentane nitriles)；And various peroxide such as benzoyl peroxide, cyclohexane peroxide, the peroxidating moon Osmanthus acyl and their mixture.

Alternatively, photoinitiator can be used for cure curable precursor composition.Exemplary photo-initiators include benzoin ether (for example, benzoin methyl ether or benzoin isopropyl ether) or the benzoin ether (for example, anisoin methyl ether) of substitution.Other examples Photoinitiator be substitution acetophenone, such as 2,2- diethoxy acetophenones or 2,2- dimethoxy -2- phenyl acetophenones (can With trade name IRGACURE 651 from BASF AG (BASF Corp.) (Ludwigshafen, Germany (Ludwigshafen, Germany)) commercially available, or with trade name ESACURE KB-1 from Sartomer (Pennsylvanian Ai Kesi )) commercially available.Other illustrative photoinitiator be substitution α -one alcohol (such as 2- methyl -2- hydroxypropiophenonepreparations), Aromatics sulfonic acid chloride (such as 2- naphthalene sulfonyl chlorides) and photolytic activity oxime (such as 1- phenyl -1,2- propanedione -2- (O- ethoxy carbonyls) Oxime).Other suitable photoinitiators include, such as 1- hydroxycyclohexylphenylketones (IRGACURE 184), bis- (2,4,6- front threes Base benzoyl) phenyl phosphine oxide (IRGACURE 819), 1- [4- (2- hydroxy ethoxies) phenyl] -2- hydroxy-2-methyls -1- third Alkane -1- ketone (IRGACURE 2959), 2- benzyl -2- dimethylaminos -1- (4- morphlinophenyls) butanone (IRGACURE 369), 2- methyl-1s-[4- (methyl mercapto) phenyl] -2- morpholino propyl- 1- ketone (IRGACURE 907) and 2- hydroxy-2-methyls - 1- phenyl propyl- 1- ketone (DAROCUR 1173).

Chain-transferring agent

Despite optional, curable precurser composition may include chain-transferring agent to control point of the elastomeric material of gained Son amount.The example of available chain-transferring agent include but not limited to carbon tetrabromide, alcohol, mercaptan such as isooctyl thioglycolate and it Mixture.If used, then polymerizable mixture may include the total weight based on curable precurser composition, at most The chain-transferring agent of 0.5 weight.For example, polymerizable mixture may include 0.01 to 0.5 weight %, 0.05 to 0.5 weight % or The chain-transferring agent of 0.05 to 0.2 weight %.

Other optional additives

The PSA provided also may include one or more another in addition to hollow non-porous particle packing material as described above Outer filler.Such packing material can add further to and can consolidate before or after being compounded with hollow non-porous particle packing material Change in precursor composition.

The typical case that can be used for the packing material of this paper includes but not limited to expand pearlite, microsphere, inflatable micro- Sphere, spheres of ceramic, zeolite, clay filler, bead, hollow inorganic pearl, silica-based filler, hydrophobic silica class Filler, hydrophilic silicon oxides class filler, pyrogenic silica, fiber (especially glass fibre, carbon fiber, graphite fibre, Silicon dioxide fibre, ceramic fibre), conductive and/or conductive particle and any combination of them.

In the specific aspect according to the PSA components of the disclosure, the second psa layer and/or third psa layer may also include hollow Non-porous particulate filler, wherein the surface of hollow non-porous particulate filler is preferably provided with hydrophobic surface modification.Can advantageously it make With such filler to increase the mechanical stability of PSA components and can also increase its shearing force and peeling force tolerance.

Pyrogenic silica can advantageously be applied in combination with above-mentioned hollow non-porous particulate filler.

For those skilled in the art, it is evident that, other additives can be optionally included in PSA groups To realize any desired characteristic in any layer of part.Such additives, including it is pigment, toughener, reinforcing agent, fire retardant, anti- Oxidant and various stabilizers.

Polymerization

PSA composition can be prepared by a variety of conventional radical polymerization methods, these methods include that polymerisation in solution, ontology are poly- Close (that is, on a small quantity or without solvent), dispersin polymerization, emulsion polymerization and suspension polymerization.Specific method used It may depend on the use of final PSA article or component.The reaction product of curable precurser composition can be random copolymer, block Copolymer or some mixed architectures.

Based on polymerization used, curable precurser composition may include organic solvent can be free of or substantially free of Organic solvent.Based on context, " solvent is substantially free of an organic " to can refer to, based on the weight meter of curable precurser composition, have The amount of solvent is less than 5 weight %, is less than 4 weight %, is less than 3 weight %, is less than 2 weight % or is less than 1 weight Measure %.If curable precurser composition includes organic solvent, the amount is generally selected to provide desired viscosity.Properly The example of organic solvent include but not limited to methanol, tetrahydrofuran, ethyl alcohol, isopropanol, heptane, acetone, methyl ethyl ketone, second Sour methyl esters, ethyl acetate, toluene, dimethylbenzene, ethylene glycol alkyl ether and any combination of them or mixture.

It is preparing for according to the one of the curable precurser compositions of one or more psa layers of the PSA components of the disclosure In a little methods, including the curable precurser composition of monomer is partially polymerized, to which its viscosity to be increased to the viscosity of viscous paste. In general, principal monomer and other optional monomers are mixed with a part for radical polymerization initiator.According to the initiation of addition The type of agent usually exposes the mixture under actinic radiation or heating, so that monovalence monomer is (that is, not with single ethylenic bond The monomer of saturated group) it is partially polymerized.Then, can pulp-like part be added in any nubbin of crosslinking agent and initiator to gather In the material of conjunction.It, can also be by particulate filler and optionally tackifier and/or plasticizer and partially polymerized material in this stage Combination.The mixture of gained can be easier as coating composition to be applied to carrier (for example, release liner) or another layer (example Such as, polymer foam layer) on.Then, coat can be exposed to actinic radiation (when there are photoinitiator) or heat (works as presence When thermal initiator).It is exposed to actinic radiation or heat typically results in the further anti-of curable precurser composition in coating composition It answers.

The PSA provided can have the storage modulus for being less than 300,000 Pascals at 25 DEG C.In some embodiments In, the storage modulus of PSA is 000 Pascal, most 100,000 Pascals, most 50,000 Paasches most 200 at 25 DEG C Card or most 25,000 Pascals.In some embodiments, storage modulus can be most 10 at 25 DEG C, 000 Pascal, Most 9,000 Pascals, most 8,000 Pascals or most 7,500 Pascals.

Manufacturing method

Present disclosure also relates to a kind of methods preparing the PSA components including at least one psa layer, and the method includes following Step：

A) by (methyl) alkyl acrylate, hollow non-porous particulate filler and include hydrophobicity alkoxy silane or hydrophobic Property organofunctional polysiloxane (or their mixture) surface modifier mixing, to provide curable precurser composition, And lead to the surface for the hollow non-porous particulate filler that there is hydrophobic surface to be modified；And

B) curable precurser composition is made to be cured to provide at least one psa layer.

According to the method for preparing PSA components specific aspect, the Liquid precursor of the first psa layer is deposited on substrate On, then cure, preferably with actinic radiation, electron beam irradiation or passes through heat cure.

According to the method illustrative aspect, the first psa layer and the second psa layer and/or the 3rd PSA is prepared separately Layer, is then laminated each other.

According to the method alternative illustrative aspect, before curing, by the second psa layer and/or third psa layer Liquid precursor be superimposed upon in the Liquid precursor of the first psa layer, specifically with actinic radiation such as UV, γ (gamma) or electronics Beam radiates or is cured by heat cure.The method is in International Patent Publication No. W 2011/094385 (Kuehneweg et al.) There is detailed description.

However, the generation of PSA components is not limited to preceding method.For example, PSA components can by coextrusion, it is solvent-based Method or combination thereof and generate.

Using

The PSA components of the disclosure can be coated or any of to be otherwise applied to a variety of substrates upper is glued with generating The product of mixture coating.Potential substrate is not particularly limited.Substrate can be flexible or not bending, and by polymer material, Glass or ceramic material, metal or combination thereof are formed.Suitable polymeric substrates include but not limited to polymer film such as By those of following material preparation：Polypropylene, polyethylene, polyvinyl chloride, polyester (polyethylene terephthalate or poly- naphthalene two Formic acid glycol ester), makrolon, poly- (methyl) methyl acrylate, cellulose acetate, cellulose triacetate and ethyl it is fine Dimension element.Foam-back can be used.The example of other substrates includes but not limited to metal such as stainless steel, metal or metal oxide The polymer material of coating, the glass etc. of metal or metal oxide-coated.

The PSA components of the disclosure can be used in conventionally known any product using this class component, such as label, band, Direction board, cover, label mark, display unit, touch tablet etc..It is also envisaged that flexible backings' material with microreplicated surface Material.

It can be used and be modified as that PSA components are coated/are applied in substrate suitable for any Conventional application techniques of particular substrate. For example, PSA components can be applied by the method for such as roller coating, flow coat, dip-coating, spin coating, spraying, blade coating and pressing mold coating etc Add/coat to various solid substrates.The thickness that these various painting methods allow PSA components can be changed is placed in substrate, from And allow the wider use scope of component.

The PSA components provided can form strong bonding with low-surface-energy (LSE) substrate and bond.Such substrate includes poly- third Alkene, polyethylene (for example, high density polyethylene (HDPE) or HDPE), polyacrylic blend (for example, PP/EPDM, TPO).Other substrates Also can have being arranged due to the residue (such as oily residue) or film (such as paint) on different base surface There is low-surface-energy characteristic.

The use of the PSA provided is not limited to low-surface-energy substrate.PSA components can be bonded to middle surface energy well (MSE) substrate, such as polyamide 6 (PA6), ABS, PC/ABS blend, PC, PVC, PA, PUR, TPE, POM, polyphenyl second Alkene, poly- (methyl methacrylate), varnish coat surface, in particular for the vehicles of similar automobile varnish coat or For the coated surface of commercial Application and the composite material of like fibrous reinforced plastics.

The PSA components provided can also be provided and higher surface energy (HSE) substrate, such as ceramics, glass and metal Strong bonding bond.

Therefore, present disclosure also relates to PSA components as described above for being bonded to low-surface-energy substrate, middle surface energy substrate And/or the purposes of high surface energy substrate.

The substrate that PSA components can be applied in generally depends on application at hand.For example, can by PSA components, especially by Its second and/or third psa layer is applied to articles of sheet material (for example, decorative image and reflection product), label paper and band Backing.In addition, PSA components can be applied directly to other substrates such as metal decking (such as vehicle panels) or windowpane On so that another substrate or object could attach on panel or window.Therefore, the PSA components of the disclosure can be used in particular for motor vehicle Process industry (such as attachment of exterior trim part or for sealing strip), building industry or solar panels building industry.

Therefore, present disclosure also relates to PSA components as described above to be used for commercial Application, be used specifically as building and machine The purposes of the acrylic foam band of motor-car application.

PSA components can also the forms of PSA transfer bands provide, wherein at least one layer of of PSA components is arranged anti-sticking For being applied to permanent substrate afterwards on liner.PSA components are alternatively arranged as single side coated strip or dual coating band Form provides, and wherein PSA components are permanently arranged on backing.Backing can be by plastics (for example, polypropylene, including twin shaft take To polypropylene, vinyl, polyethylene, polyester such as polyethylene terephthalate), non-woven fabric (for example, paper, cloth, Non-woven scrim), metal foil and foam (for example, polyacrylic, polyethylene, polyurethane, neoprene) be made.It is poly- Closing object foam can be commercially available from various suppliers, such as 3M companies, Voltek and Sekisui Chemical Co., Ltd.Polymer Froth bed may be molded to the thin slice being coextruded with PSA components on the one or both sides of polymer foam layer, or can be by PSA groups Part is laminated thereon.

When by PSA component laminations in substrate, it may be desirable to handle the surface of substrate to improve adhesiveness.Such processing The property of material and the property of substrate in PSA components is typically based on to be selected, and include priming paint and surface be modified (for example, Sided corona treatment and surface abrasion).

For single side band, PSA components are administered on a surface of back lining materials and by suitable adhesive It is applied on the apparent surface of back lining materials.Adhesive is known, and includes such as siloxanes, polyolefin, poly- The material of carbamate and polyacrylic.For the band of dual coating, PSA components are administered to back lining materials A surface on, and PSA components are arranged on the apparent surface of back lining materials.The band of dual coating is usually supported on anti- On viscous liner.

It is not intended in detail, non-limiting embodiments in addition are listed below：

1. a kind of curable precurser composition for contact adhesive, the curable precurser composition include：(first Base) alkyl acrylate；Hollow non-porous particulate filler；And it is poly- comprising hydrophobicity alkoxy silane or hydrophobicity functional organic The surface modifier of siloxanes.

2. the curable precurser composition according to embodiment 1, wherein the hollow non-porous particulate filler is by hollow Glass microsphere forms.

3. the curable precurser composition according to embodiment 1 or 2, wherein the surface modifier has followingization Learn structure：

(R¹-O)_m(R²)_pSi-[(O-Si(OR¹)_q(R²)_2-q)_x-Si(O-R¹)_m(R²)_3-m]_r,

Wherein R¹It independently is alkyl, R²Hydrophobic parts independently are, m is in the range of 0 to 3, ranges of the p 0 to 3 Interior, for q in the range of 0 to 2, for r in the range of 0 to 4, for x in the range of 0 to 9, wherein summation m+p+r is equal to 4 and wherein There are at least one R¹With at least one R²。

4. the curable precurser composition according to embodiment 3, wherein R¹With 1 to 6 carbon atom.

5. the curable precurser composition according to embodiment 4, wherein R¹With 1 to 4 carbon atom.

6. the curable precurser composition according to embodiment 5, wherein R¹With 1 or 2 carbon atom.

7. the curable precurser composition according to any one of embodiment 3-6, wherein the hydrophobic parts R² Selected from saturation, unsaturation, straight chain, branch and cyclic alkyl and combination thereof.

8. the curable precurser composition according to embodiment 7, wherein the hydrophobic parts have 1 to 100 Carbon atom.

9. the curable precurser composition according to embodiment 8, wherein the hydrophobic parts have 1 to 50 carbon Atom.

10. the curable precurser composition according to embodiment 9, wherein the hydrophobic parts have 1 to 30 Carbon atom.

11. the curable precurser composition according to embodiment 10, wherein the hydrophobic parts have 1 to 25 Carbon atom.

12. the curable precurser composition according to any one of embodiment 3-11, wherein R²Independently selected from：First Base, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, ten Tetraalkyl, pentadecyl, cetyl, heptadecyl, octadecyl, nonadecyl, eicosyl, its fluorinated derivatives, with And 13 fluoro- 1,2,2,2- tetrahydrochysenes octyl.

13. the curable precurser composition according to embodiment 12, wherein R²Independently selected from：Methyl, propyl, just Octyl and cetyl.

14. a kind of pressure-sensitive adhesive composition, the pressure-sensitive adhesive composition is by making according to embodiment 1 to 13 Any one of described in curable precurser composition solidification and obtain.

15. a kind of pressure-sensitive adhesive assembly, the pressure-sensitive adhesive assembly include：Back sheet；And first pressure-sensitive adhesion Oxidant layer, first pressure sensitive adhesive layer include the pressure-sensitive adhesion according to embodiment 14 being arranged on the back sheet Agent composition.

16. according to the pressure-sensitive adhesive assembly described in embodiment 15, wherein first pressure sensitive adhesive layer is polymerization Object froth bed.

17. the pressure-sensitive adhesive assembly according to embodiment 15 or 16 further includes that setting is pressure-sensitive viscous described first The second pressure sensitive adhesive layer in one or two main surface of mixture layer.

18. it is table sheath core multi-layer pressure-sensitive adhesive component according to the pressure-sensitive adhesive assembly described in embodiment 17 Form, wherein first pressure sensitive adhesive layer is the sandwich layer of the multi-layer pressure-sensitive adhesive component, and described second Pressure sensitive adhesive layer is the epidermis of the multi-layer pressure-sensitive adhesive component.

19. the pressure-sensitive adhesive assembly according to any one of embodiment 15 to 18, wherein described second is pressure-sensitive viscous Mixture layer include polymeric matrix material, the polymeric matrix material be selected from polyacrylate, polyurethane, polyolefin, polyamine, Polyamide, polyester, polyethers, polyisobutene, polystyrene, polyethylene, polyvinylpyrrolidone, natural rubber, synthetic rubber, with And their copolymer and blend.

20. according to the pressure-sensitive adhesive assembly described in embodiment 19, wherein second pressure sensitive adhesive layer includes poly- Acrylate, major monomeric compoent include (methyl) alkyl acrylate of linear chain or branched chain.

21. according to the pressure-sensitive adhesive assembly described in embodiment 20, wherein second pressure sensitive adhesive layer includes tool There are the nonpolar linear of linear or branched alkyl group group or (methyl) alkyl acrylate of branch.

22. according to the pressure-sensitive adhesive assembly described in embodiment 21, wherein the linear or branched alkyl group group has 1 To 32 carbon atoms.

23. according to the pressure-sensitive adhesive assembly described in embodiment 22, wherein the linear or branched alkyl group group has 4 To 20 carbon atoms.

24. according to the pressure-sensitive adhesive assembly described in embodiment 23, wherein the linear or branched alkyl group group has 4 To 12 carbon atoms.

25. a kind of method preparing contact adhesive, the method includes：By (methyl) alkyl acrylate, hollow nothing Hole particulate filler and surface modifier comprising hydrophobicity alkoxy silane or hydrophobicity organofunctional polysiloxane are mixed It closes, to provide curable precurser composition；And the curable precurser composition is made to be cured to provide the contact adhesive.

26. according to the method described in embodiment 25, wherein the total weight gauge based on the precursor composition, the table The amount of face modifying agent is 0.05 weight % to 3 weight %.

27. according to the method described in embodiment 26, wherein the total weight gauge based on the precursor composition, the table The amount of face modifying agent is 0.1 weight % to 2 weight %.

28. according to the method described in embodiment 27, wherein the total weight gauge based on the precursor composition, the table The amount of face modifying agent is 0.3 weight % to 1.5 weight %.

29. according to the method described in any one of embodiment 25-28, wherein based on the curable precurser composition The amount of total weight gauge, the hollow non-porous particulate filler is 6 weight % to 14 weight %.

30. according to the method described in embodiment 29, wherein the total weight gauge based on the curable precurser composition, The amount of the hollow non-porous particulate filler is 8 weight % to 13 weight %.

31. according to the method described in embodiment 30, wherein the total weight gauge based on the curable precurser composition, The amount of the hollow non-porous particulate filler is 10 weight % to 12 weight %.

Embodiment：

By following non-limiting embodiment, the objects and advantages of the disclosure are further illustrated, but in these embodiments The specific material and its amount of middle reference and other conditions and details are not construed as the improper restriction to the disclosure.

Unless otherwise stated, all numbers, percentage, ratio etc. in the rest part of embodiment and this specification It is by weight.

Table 1：Material

Test method

Ribbon performance (" 90 ° of peel tests ")

Using with aqueous isopropanol (50:50 volume/volumes) wetting SURPASS face tissues (Kimberly-Clark company (Kimberly-Clark)) then clean substrate makes it dry.From (1 inch of cutting of web item on each pressure-sensitive adhesive assembly × 4 inches ,~2.5cm ×~10cm), and anodization aluminium foil is used to be placed as backing and by another face on one face Onto the surface primed, then pushed twice under with 15 pounds of 12 inches per minute (~30cm) mobile (6.8kg) rollers. 90 ° of peel strengths are assessed after standing 72 hours at room temperature, and anodization is pulled with 12 inches per minute (~30cm) perpendicular to substrate Aluminium foil backing.Average peel force records together with failure mode.During failure mode " fs " instruction test in foam band Cohesional failure, " cp " mean the band totally removed from surface and the band not cohesional failure, and " mixing dduring test Object " indicates to observe the mixture of fs and cp failure modes dduring test.The list of bond properties test substrate is immediately rear：

Bond properties test substrate

Band keeps power (" static shear test ")

Stainless steel faceplate SURPASS face tissues (Kimberly-Clark company) are cleaned five times, wet with solvent is used；First With ethyl acetate, aqueous isopropanol (50 is then used:50 volume/volumes), then use acetone three times；Then it makes it dry. Cutting of web item (0.5 inch × 1 inch ,~1.3cm ×~2.5cm) from each pressure-sensitive adhesive assembly is mounted on two Between flat polishing stainless steel panel, is pushed 15 minutes in 1kg mass, component is overhang 158 from a stainless steel faceplate In ℉ (70 DEG C) baking oven, so that it is balanced 10 minutes, 500g mass is then attached to another panel and starts timer.Note Record time to rupture and failure mode.The bonding remained after 10,000 minutes is completely removed and is expressed as>10,000 points Clock.

Preparation example 1 (PE-1)：It is used to prepare the pre-composition of curable precurser composition

The partially polymerized slurries of IOA/AA are prepared in the following manner：96 parts of IOA, 4 parts of AA and 0.04 part of IRG651 are mixed It closes；Make mixture and headspace inerting with nitrogen；Stir mixture and in 0.3mW/cm²Lower irradiation is until reach about The viscosity of 2500cps；Then it is quenched with air purging.P-125 is prepared separately in the EHA of weight exists by being dissolved in P-125 etc. 50 weight % solution in EHA.10 weights of the HDDA in EHA are prepared separately by the way that a HDDA to be diluted in nine parts of EHA Measure % solution.The ingredient listed in merging table 2, and mildly mix until uniformly.PE-1 include 0.08phr HDDA, 0.20phr IRG651 and 12.5phr P-125.Term " phr " refers to " total number of every hundred weight IOA+EHA+AA "； In this case, IOA+EHA+AA is IOA/AA slurries, EHA, AA, 0.5*P-125 solution weight and 0.9*HDDA solution The summation of weight.

Table 2：The ingredient of PE-1。

Ingredient	It measures (gram)
		IOA/AA slurries	156.48
EHA	29.30
		AA	2.34
HDDA (10 weight %, in EHA)	1.72
		IRG651	0.43
P-125 (50 weight %, in EHA)	53.75
		PENN PIGMENT	0.43

Preparation example 2 (PE-2)：It is used to prepare the pre-composition of curable precurser composition

PE-2 is prepared according to PE-1, unlike with etc. weigh (188.12 grams) the partially polymerized slurries of IOA/EHA/AA replace First three ingredient (IOA/AA slurries, EHA, AA).Partially polymerized IOA/EHA/AA slurries are prepared in the following manner：By 79.8 Part IOA, 15.6 parts of EHA, 4.6 parts of AA and 0.04 part of IRG651 mixing；Mixture and headspace is set to become inerting with nitrogen； Stir mixture and in 0.3mW/cm²Lower irradiation is until reach the viscosity of about 2500cps；Then it is quenched with air purging.

Preparation example 3 (PE-3)：The preparation of contact adhesive epidermis

According to high T_gThe US 2014/0044457 of copolymer HTG1 prepares to prepare high T_gAcrylic copolymer.According to low T_g Method prepared by the US 2014/0044457 of acrylic size (S1-S5) prepares low T_gAcrylic size, but use 83.75 parts of EHA, 3.75 parts of AA and 12.50 part of IBOA.PE-3 contact adhesives epidermis is implemented according to US 2015/0044457 Prepared by example 6, only replace P140 with P-125 and use above high T of ratio shown in table 3_gAcrylic copolymer, more than Low T_gAcrylic size and P-125.

Table 3：The ingredient of PE-3

Embodiment 1 (EX-1)：Include the curable precurser composition of oligosiloxane modifying agent

The amount of ingredient is summarized in table 4.Therefore, added into 56.85 grams of the parts PE-1 5.0 grams of AEROSIL R972 and 0.70 gram of DS-9896, and with saw-toothed blade by this mixture be vigorously stirred three minutes until warm (about 43 DEG C) and uniformly, so 8.00 grams of K15 glass envelopes are added under mild mixing afterwards.

Table 4：

Comparative example 1 (CE-1)

The amount of ingredient is summarized in table 4.For CE-1, the AEROSIL R972 of 5.0g are added into 56.85 grams of PE-1, and And with saw-toothed blade this mixture is vigorously stirred three minutes until warm (about 43 DEG C) and uniformly, then under mild mixing plus Enter the sK15 glass envelopes of 8.00 grams of silanizations.

Comparative example 2 (CE-2)

The program is identical as CE-1, the difference is that having used K15 glass envelopes to be steeped instead of sK15 silanized glass, in table 4 Summarized.

Embodiment 2 (EX-2)：Solidification composition filling including K15 glass envelopes and oligosiloxane modifying agent

By the gained mixture from EX-1, slowly rolling overnight, then casts in silicon with 43 mils (~1.1mm) thickness Between poly- (ethylene glycol terephthalate) (PET) release liner pad film of oxygen alkane coating.Casting mixture is then existed with UV light 1.5mW/cm²Lower irradiation 190 seconds, then in 8.0W/cm²Lower irradiation 230 seconds.Then the solidification core of gained is laminated on both sides (after PET release liners are removed) to PE-3 contact adhesives epidermis (in PET release liners prepare).90 ° of strippings are surveyed Test result is summarized in table 5.Static shear test result is summarized in table 6.

Comparative example 3 (CE-3)：Including sK15 glass envelopes, without the solidification composition filling of modifying agent

The gained mixture from CE-1 is handled according to the process of EX-1.90 ° of peel test results are summarized in table 5.

Comparative example 4 (CE-4)：Including K15 glass envelopes, without the solidification composition filling of modifying agent

The gained mixture from CE-2 is handled according to the process of EX-1.90 ° of peel test results (average value of three-wheel) It is summarized in table 5.

Table 5：

Table 6：

90 ° of peel tests that EX-2 is assessed in additional substrate, are as a result summarized in table 7.

Table 7：90 ° peel tests and failure mode of the EX 2 in additional substrate

Embodiment 3 to 5 (EX-3 to EX-5)：Curable precurser composition including oligosiloxane modifying agent

For each in EX-3 to EX-5, it then follows the program of EX-1, the difference is that use PE-2 as pre-composition, and And change the amount of DS-9896 also according to the relative quantity of listed material in table 8.

Table 8：

Embodiment 6 to 8 (EX-6 to EX-8)

For each in EX-3 to EX-5, it then follows the program of EX-2 obtains the cured lamination sample with PSA epidermises Product EX-6 to EX-8.Therefore, EX-6 is generated by EX-3, and EX-7 is generated by EX-4, and EX-8 is generated by EX-5.90 ° of strippings are surveyed Test result is summarized in table 9.Static shear test result is summarized in table 10.

Table 9：

Table 10：The static shear test result (stainless steel) of EX-6 to EX-8

Embodiment 9 (EX-9)

EX-7 (since the curable precurser composition of EX-4) is repeated, the difference is that with there is same binder but passing through The table prepared on brown paper (PCK) liner (instead of the polyester liner through siloxane treated) of the polyethylene coating of siloxane treated Skin replaces PE-3 contact adhesive epidermises.

Table 11：

Embodiment 10 to 14 (EX-10 to EX-14)：Curable precurser composition including silane

The additional embodiment that program used in EX-1 prepares curable precurser composition is followed, the difference is that using premix Object PE-2 replaces PE-1, and replaces DS-9896 using silane DS-OCTMO or DS-9116.Amount is summarized in table 12.

Table 12：

Embodiment 15 to 19 (EX-15 to EX-19)

For each in EX-10 to EX-14, it then follows the program of EX-2 obtains the cured lamination with PSA epidermises Sample EX-15 to EX-19.Therefore, EX-15 is generated by EX-10, and EX-16 is generated by EX-11, and EX-17 is generated by EX-12, EX- 18 are generated by EX-13, and EX-19 is generated by EX-14.90 ° of peel test results are summarized in table 13.Shearing test result is converged Always in table 14.

Table 13：

Table 14：

The bibliography of all references, patents and patent applications are in a uniform matter in the application of patent certificate achieved above It is incorporated by reference and is incorporated herein.The case where there are inconsistent or contradictions between the bibliography part being incorporated to and the application Under, the information that should be subject in preceding description.It is protected by claims to enable those skilled in the art to put into practice The disclosure of shield and the preceding description that provides should not be construed as the limitation to disclosure range, the scope of the present disclosure is by right Claim and its all equivalent forms limit.

Claims

1. a kind of curable precurser composition for contact adhesive, the curable precurser composition include：

(methyl) alkyl acrylate；

Hollow non-porous particulate filler；And

Surface modifier, the surface modifier include hydrophobicity alkoxy silane or hydrophobicity organofunctional polysiloxane.

2. curable precurser composition according to claim 1, wherein the hollow non-porous particulate filler is by hollow glass Microballoon forms.

3. curable precurser composition according to claim 1 or 2, wherein there is the surface modifier following chemistry to tie Structure：

(R¹-O)_m(R²)_pSi-[(O-Si(OR¹)_q(R²)_2-q)_x-Si(O-R¹)_m(R²)_3-m]_r,

Wherein R¹It independently is alkyl, R²Hydrophobic parts independently are, for m in the range of 0 to 3, p is in the range of 0 to 3, q In the range of 0 to 2, in the range of 0 to 4, in the range of 0 to 9, wherein summation m+p+r is equal to 4 and wherein exists x r At least one R¹With at least one R²。

4. curable precurser composition according to claim 3, wherein R¹With 1 to 4 carbon atom.

5. curable precurser composition according to claim 4, wherein R¹With 1 or 2 carbon atom.

6. the curable precurser composition according to any one of claim 3-5, wherein the hydrophobic parts have 1 to 25 carbon atoms.

7. the curable precurser composition according to any one of claim 3-6, wherein R²Independently selected from：Methyl, third Base, n-octyl and cetyl.

8. a kind of pressure-sensitive adhesive composition, the pressure-sensitive adhesive composition is by making according to any in claim 1 to 7 Described in curable precurser composition solidification and obtain.

9. a kind of pressure-sensitive adhesive assembly, the pressure-sensitive adhesive assembly include：

Back sheet；And

First pressure sensitive adhesive layer, first pressure sensitive adhesive layer include to be arranged on the back sheet according to claim Pressure-sensitive adhesive composition described in 8.

10. pressure-sensitive adhesive assembly according to claim 9, wherein first pressure sensitive adhesive layer is foam of polymers Layer.

11. pressure-sensitive adhesive assembly according to claim 9 or 10, the pressure-sensitive adhesive assembly further includes being arranged in institute State the second pressure sensitive adhesive layer in one or two main surface of the first pressure sensitive adhesive layer.

12. pressure-sensitive adhesive assembly according to claim 11 is the shape of table sheath core multi-layer pressure-sensitive adhesive component Formula, wherein first pressure sensitive adhesive layer is the sandwich layer of the multi-layer pressure-sensitive adhesive component, and it is described second pressure-sensitive viscous Mixture layer is the epidermis of the multi-layer pressure-sensitive adhesive component.

13. pressure-sensitive adhesive assembly according to claim 11 or 12, wherein second pressure sensitive adhesive layer includes poly- Acrylate, the major monomeric compoent of the polyacrylate include the linear chain or branched chain for having linear or branched alkyl group group (methyl) alkyl acrylate.

14. pressure-sensitive adhesive assembly according to claim 13, wherein the linear or branched alkyl group group has 4 to 12 A carbon atom.

15. a kind of method preparing contact adhesive, the method includes：

Have by (methyl) alkyl acrylate, hollow non-porous particulate filler and comprising hydrophobicity alkoxy silane or hydrophobicity The surface modifier of machine functional polysiloxanes mixes, to provide curable precurser composition；And

The curable precurser composition is set to be cured to provide the contact adhesive.